JP2827880B2 - Biaxially oriented thermoplastic resin film - Google Patents

Biaxially oriented thermoplastic resin film

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Publication number
JP2827880B2
JP2827880B2 JP6017499A JP1749994A JP2827880B2 JP 2827880 B2 JP2827880 B2 JP 2827880B2 JP 6017499 A JP6017499 A JP 6017499A JP 1749994 A JP1749994 A JP 1749994A JP 2827880 B2 JP2827880 B2 JP 2827880B2
Authority
JP
Japan
Prior art keywords
film
thermoplastic resin
particles
biaxially oriented
scratch resistance
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP6017499A
Other languages
Japanese (ja)
Other versions
JPH06256544A (en
Inventor
巌 岡崎
晃一 阿部
彰二 中島
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TORE KK
Original Assignee
TORE KK
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Filing date
Publication date
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Priority to JP6017499A priority Critical patent/JP2827880B2/en
Publication of JPH06256544A publication Critical patent/JPH06256544A/en
Application granted granted Critical
Publication of JP2827880B2 publication Critical patent/JP2827880B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は二軸配向熱可塑性樹脂フ
ィルムに関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a biaxially oriented thermoplastic resin film.

【0002】[0002]

【従来の技術】二軸配向熱可塑性樹脂フィルムとして
は、熱可塑性樹脂であるポリエステルにコロイド状シリ
カに起因する実質的に球状のシリカ粒子を含有せしめた
フィルムが知られている(たとえば特開昭59−171
623号公報)。
2. Description of the Related Art As a biaxially oriented thermoplastic resin film, a film in which substantially spherical silica particles derived from colloidal silica are contained in a polyester resin as a thermoplastic resin is known (for example, see Japanese Patent Application Laid-Open Publication No. 59-171
623).

【0003】[0003]

【発明が解決しようとする課題】しかし、上記従来の二
軸配向熱可塑性樹脂フィルムは、フィルムの加工工程、
たとえば包装用途における印刷工程、磁気媒体用途にお
ける磁性層塗布・カレンダー工程あるいは感熱転写用途
における感熱転写層塗布などの工程速度の増大にともな
い、接触するロールによってフィルム表面に傷がつくと
いう欠点が最近、問題となってきている。
However, the above-mentioned conventional biaxially oriented thermoplastic resin film has a film processing step,
For example, with the increase in process speeds such as the printing process in packaging applications, the application and calendering of magnetic layers in magnetic media applications, and the application of thermal transfer layers in thermal transfer applications, there has recently been the disadvantage that the film surface is scratched by the contacting rolls. Is becoming a problem.

【0004】また、上記従来の二軸配向熱可塑性樹脂フ
ィルムは高温・高湿下で、フィルムを取り扱う時に摩擦
係数が高くなり、ハンドリング性が不良になるという問
題点があった。
[0004] Further, the conventional biaxially oriented thermoplastic resin film has a problem that the coefficient of friction increases when handling the film under high temperature and high humidity, resulting in poor handling properties.

【0005】さらに、フィルムの主要な用途であるビデ
オテープは、最近、ソフト用(制作された映像作品をパ
ッケージ媒体に記録固定、複製、増製したもの)に用い
られるケースが多く、この場合、上記従来のビデオテー
プでは、「映像作品を録画する工程」でマスターテープ
から高速でダビング(記録複写)する時のS/N(シグ
ナル/ノイズ比、画質のパラメータ)の低下が大きく画
質が悪くなるという問題展も出てきている。
[0005] In addition, video tapes, which are the main applications of film, are often used for software (recorded video works fixed on a package medium, copied, and expanded) in many cases. In this case, In the above-mentioned conventional video tape, the S / N (signal / noise ratio, parameters of image quality) when dubbing (recording and copying) from the master tape at a high speed in the "step of recording a video work" is greatly reduced, and the image quality is deteriorated. A problem exhibition has also appeared.

【0006】本発明はかかる問題点を改善し、表面が傷
つきにくく(以下耐スクラッチ性という)、高温・高湿
下での摩擦係数が小さく(以下、摩擦係数という)、か
つ、ダビングによる画質(S/N)の低下が少ない(耐
ダビング性という)フィルムを提供することを課題とす
る。
The present invention has solved the above problems, has a low scratch resistance on the surface (hereinafter referred to as scratch resistance), has a small coefficient of friction under high temperature and high humidity (hereinafter referred to as a coefficient of friction), and has an image quality obtained by dubbing. It is an object of the present invention to provide a film with a small decrease in S / N (dubbing resistance).

【0007】[0007]

【課題を解決するための手段】フィルム中に含有する不
活性粒子の平均粒径がフィルム厚さの0.1〜10倍で
あって、該粒子の含有量が0.5〜50重量%であるこ
とを特徴とする厚さ0.5〜3μmの磁気記録媒体用二
軸配向熱可塑性樹脂フィルムとしたものである。
The inert particles contained in the film have an average particle size of 0.1 to 10 times the film thickness, and the content of the particles is 0.5 to 50% by weight. A biaxially oriented thermoplastic resin film for a magnetic recording medium having a thickness of 0.5 to 3 [ mu] m.

【0008】本発明を構成する熱可塑性樹脂Aはポリエ
ステル、ポリオレフィン、ポリアミド、ポリフェニレン
スルフィドなど特に限定されることはないが、特に、ポ
リエステル、中でも、エチレンテレフタレート、エチレ
ンα,β−ビス(2−クロルフェノキシ)エタン−4−
4′−ジカルボキシレート、エチレン2,6−ナフタレ
ート単位から選ばれた少なくとも一種の構造単位を主要
構成成分とする場合に耐スクラッチ性、耐ダビング性、
摩擦係数がより一層良好となるので望ましい。また、本
発明を構成する熱可塑性樹脂は結晶性、あるいは溶融時
光学異方性である場合に耐スクラッチ性、耐ダビング
性、摩擦係数がより一層良好となるのできわめて望まし
い。ここでいう結晶性とはいわゆる非晶質ではないこと
を示すものであり、定量的には結晶化パラメータにおけ
る冷結晶化温度Tccが検出され、かつ結晶化パラメー
タΔTcgが150℃以下のものである。さらに、示差
走査熱量計で測定された融解熱(融解エンタルピー変
化)が7.5cal/g以上の結晶性を示す場合に耐ス
クラッチ性、耐ダビング性、摩擦係数がより一層良好と
なるのできわめて望ましい。また、エチレンテレフタレ
ートを主要構成成分とするポリエステルの場合に耐ダビ
ング性と耐スクラッチ性がより一層良好となるので特に
望ましい。なお、本発明を阻害しない範囲内で、2種以
上の熱可塑性樹脂を混合しても良いし、共重合ポリマを
用いても良い。
The thermoplastic resin A constituting the present invention is not particularly limited, such as polyester, polyolefin, polyamide, and polyphenylene sulfide. Particularly, polyester, especially, ethylene terephthalate, ethylene α, β-bis (2-chloro) Phenoxy) ethane-4-
When at least one structural unit selected from 4'-dicarboxylate and ethylene 2,6-naphthalate units is used as a main component, scratch resistance, dubbing resistance,
This is desirable because the coefficient of friction is further improved. Further, the thermoplastic resin constituting the present invention is extremely desirable when it is crystalline or has optical anisotropy when melted, because the scratch resistance, the dubbing resistance and the friction coefficient are further improved. The term "crystallinity" as used herein means that it is not amorphous, and quantitatively, the cold crystallization temperature Tcc in the crystallization parameters is detected, and the crystallization parameter ΔTcg is 150 ° C. or less. . Further, when the heat of fusion (change in enthalpy of fusion) measured by a differential scanning calorimeter shows crystallinity of 7.5 cal / g or more, scratch resistance, dubbing resistance, and coefficient of friction are further improved, which is extremely desirable. . Further, in the case of a polyester containing ethylene terephthalate as a main component, it is particularly desirable because the dubbing resistance and the scratch resistance are further improved. Note that two or more kinds of thermoplastic resins may be mixed or a copolymer may be used as long as the present invention is not impaired.

【0009】本発明の熱可塑性樹脂A中の不活性粒子
は、フィルム中での粒径比(粒子の長径/短径)が1.
0〜1.3の粒子、特に、球形状の粒子の場合に耐スク
ラッチ性がより一層良好となるので望ましい。
The inert particles in the thermoplastic resin A of the present invention have a particle size ratio (particle long diameter / short diameter) of 1.
Particles having a particle size of 0 to 1.3, particularly spherical particles, are desirable because scratch resistance is further improved.

【0010】また、本発明の熱可塑性樹脂A中の不活性
粒子はフィルム中での単一粒子指数が0.7以上、好ま
しくは0.9以上である場合に耐スクラッチ性、耐ダビ
ング性がより一層良好となるので特に望ましい。
The inert particles in the thermoplastic resin A of the present invention have scratch resistance and dubbing resistance when the single particle index in the film is 0.7 or more, preferably 0.9 or more. It is particularly desirable because it is even better.

【0011】また、本発明の熱可塑性樹脂A中の不活性
粒子は、フィルム中での相対標準偏差が0.6以下、好
ましくは0.5以下の場合に耐スクラッチ性、耐ダビン
グ性がより一層良好となるので望ましい。
The inert particles in the thermoplastic resin A of the present invention have better scratch resistance and dubbing resistance when the relative standard deviation in the film is 0.6 or less, preferably 0.5 or less. It is desirable because it becomes even better.

【0012】本発明の熱可塑性樹脂A中の不活性粒子の
種類は特に限定されないが、上記の好ましい粒子特性を
満足するにはアルミナ珪酸塩、1次粒子が凝集した状態
のシリカ、内部析出粒子などは好ましくなく、コロイダ
ルシリカに起因する実質的に球形のシリカ粒子、架橋高
分子による粒子(たとえば架橋ポリスチレン)などがあ
るが、特に10重量%減量時温度(窒素中で熱重量分析
装置島津TG−30Mを用いて測定。昇温速度20℃/
分)が380℃以上になるまで架橋度を高くした架橋高
分子粒子の場合に耐スクラッチ性、耐タビング性がより
一層良好となるので特に望ましい。なお、コロイダルシ
リカに起因する球形シリカの場合にはアルコキシド法で
製造された、ナトリウム含有量が少ない、実質的に球形
のシリカの場合に耐スクラッチ性がより一層良好となる
ので特に望ましい。しかしながら、その他の粒子、例え
ば炭酸カルシウム、二酸化チタン、アルミナ等の粒子で
もフィルム厚さと平均粒径の適切なコントロールにより
十分使いこなせるものである。
The type of inert particles in the thermoplastic resin A of the present invention is not particularly limited, but alumina silicate, silica in which primary particles are agglomerated, and internally precipitated particles are required to satisfy the above preferable particle characteristics. And the like are not preferred, and include substantially spherical silica particles resulting from colloidal silica, particles of a crosslinked polymer (for example, crosslinked polystyrene), and the like. In particular, the temperature at the time of a 10% weight loss (nitrogen thermogravimetric analyzer Shimadzu TG) Measured using −30 M. Heating rate 20 ° C. /
In particular, in the case of the crosslinked polymer particles having a high degree of crosslink until the temperature reaches 380 ° C. or higher, the scratch resistance and the tabbing resistance are further improved. In the case of spherical silica originating from colloidal silica, it is particularly desirable to use a substantially spherical silica produced by the alkoxide method and having a low sodium content, since the scratch resistance is further improved. However, other particles, such as particles of calcium carbonate, titanium dioxide, alumina, etc., can be sufficiently used by appropriately controlling the film thickness and the average particle size.

【0013】本発明の熱可塑性樹脂A中の不活性粒子の
結晶化促進係数は特に限定されないが、−15〜15
℃、好ましくは−5℃〜10℃の場合に、耐スクラッチ
性がより一層良好となるので特に望ましい。
The crystallization promoting coefficient of the inert particles in the thermoplastic resin A of the present invention is not particularly limited, but may be from -15 to 15
C., and more preferably, -5.degree. C. to 10.degree. C., because scratch resistance is further improved.

【0014】不活性粒子の大きさは、フィルム中での平
均粒径がフィルム厚さの0.1〜10倍、好ましくは
0.5〜5倍、さらに好ましくは1.1〜3倍の範囲で
あることが必要である。平均粒径/フィルム厚さ比が上
記の範囲より小さいと耐スクラッチ性、摩擦係数が不良
となり、逆に大きくても耐スクラッチ性、耐ダビング
性、摩擦係数が不良となるので好ましくない。
The size of the inert particles is such that the average particle size in the film is 0.1 to 10 times, preferably 0.5 to 5 times, more preferably 1.1 to 3 times the film thickness. It is necessary to be. If the average particle diameter / film thickness ratio is smaller than the above range, the scratch resistance and the coefficient of friction become poor, and if the ratio is large, the scratch resistance, the dubbing resistance and the coefficient of friction become unfavorable.

【0015】また熱可塑性樹脂A中の不活性粒子のフィ
ルム中での平均粒径(直径)が0.007〜0.5μ
m、好ましくは0.02〜0.45μmの範囲である場
合に、耐スクラッチ性、耐ダビング性、摩擦係数がより
一層良好となるので望ましい。本発明の熱可塑性樹脂A
中の不活性粒子の含有量は0.5〜50重量%、好まし
くは1〜30重量%、さらに好ましくは2〜15重量%
であることが必要である。不活性粒子の含有量が上記の
範囲より少なくても、逆に大きくても耐スクラッチ性が
不良となるので好ましくない。
The average particle size (diameter) of the inert particles in the thermoplastic resin A in the film is 0.007 to 0.5 μm.
m, preferably in the range of 0.02 to 0.45 μm, because the scratch resistance, the dubbing resistance and the coefficient of friction are further improved. Thermoplastic resin A of the present invention
The content of inert particles therein is 0.5 to 50% by weight, preferably 1 to 30% by weight, more preferably 2 to 15% by weight.
It is necessary to be. If the content of the inert particles is less than the above range, or if the content is large, the scratch resistance becomes poor, which is not preferable.

【0016】本発明フィルムは上記熱可塑性樹脂Aと不
活性粒子からなる組成物を主要成分とするが、本発明の
目的を阻害しない範囲内で、他種ポリマをブレンドして
もよいし、また酸化防止剤、熱安定剤、滑剤、紫外線吸
収剤などの有機添加剤が通常添加される程度添加されて
いてもよい。
The main component of the film of the present invention is a composition comprising the above-mentioned thermoplastic resin A and inert particles. Other types of polymers may be blended as long as the object of the present invention is not impaired. Organic additives such as antioxidants, heat stabilizers, lubricants and ultraviolet absorbers may be added to the extent that they are usually added.

【0017】本発明フィルムは上記組成物を二軸配向せ
しめたフィルムである。一軸あるいは無配向フィルムで
は耐スクラッチ性が不良となるので好ましくない。この
配向の程度は特に限定されないが、高分子の分子配向の
程度の目安であるヤング率が長手方向、幅方向ともに3
50kg/mm2 以上である場合に耐スクラッチ性がよ
り一層良好となるのできわめて望ましい。分子配向の程
度の目安であるヤング率の上限は特に限定されないが、
通常、5000kg/mm2 程度が製造上の限界であ
る。
The film of the present invention is a film in which the above composition is biaxially oriented. A uniaxial or non-oriented film is not preferred because scratch resistance becomes poor. Although the degree of this orientation is not particularly limited, the Young's modulus, which is a measure of the degree of molecular orientation of the polymer, is 3 in both the longitudinal and width directions.
When it is 50 kg / mm 2 or more, scratch resistance is further improved, which is very desirable. The upper limit of the Young's modulus, which is a measure of the degree of molecular orientation, is not particularly limited,
Usually, about 5000 kg / mm 2 is the manufacturing limit.

【0018】また、本発明フィルムは、ヤング率が上記
範囲内であっても。フィルムの厚さ方向の一部分、例え
ば、表層付近のポリマ分子の配向が無配向、あるいは、
一軸配向になっていない、すなわち、厚さ方向の全部分
の分子配向が二軸配向である場合に耐スクラッチ性、耐
ダビング性、摩擦係数がより一層良好となるので特に望
ましい。
The film of the present invention may have a Young's modulus within the above range. Part of the thickness direction of the film, for example, the orientation of the polymer molecules near the surface layer is non-oriented, or
When the film is not uniaxially oriented, that is, when the molecular orientation of all portions in the thickness direction is biaxially oriented, scratch resistance, dubbing resistance, and friction coefficient are further improved, which is particularly desirable.

【0019】特に、アッベ屈折率計、レーザーを用いた
屈折率計、全反射レーザーラマン法などによって測定さ
れる分子配向が、表面、裏面ともに二軸配向である場合
に耐スクラッチ性、耐ダビング性、摩擦係数がより一層
良好となるので特に望ましい。
In particular, when the molecular orientation measured by an Abbe refractometer, a refractometer using a laser, a total reflection laser Raman method or the like is biaxial on both the front surface and the back surface, scratch resistance and dubbing resistance are obtained. This is particularly desirable because the coefficient of friction is further improved.

【0020】さらに熱可塑性樹脂Aが結晶性ポリエステ
ルであり、これを主成分とする本発明フィルムの表面の
全反射ラマン結晶化指数が20cm-1以下、好ましくは
18cm-1以下、さらに17cm-1以下の場合に耐スク
ラッチ性、耐ダビング性、摩擦係数がより一層良好とな
るのできわめて望ましい。
Further, the thermoplastic resin A is a crystalline polyester, and the total reflection Raman crystallization index on the surface of the film of the present invention containing this as a main component is 20 cm -1 or less, preferably 18 cm -1 or less, and more preferably 17 cm -1. In the following cases, scratch resistance, dubbing resistance, and coefficient of friction are further improved, which is extremely desirable.

【0021】本発明の熱可塑性樹脂Aを主成分とするフ
ィルムの二次イオンマススペクトルによって測定される
表層粒子濃度比は特に限定されないが、1/10以下、
特に1/50以下である場合の摩擦係数、耐スクラッチ
性がより一層良好となるので特に望ましい。
The surface particle concentration ratio of the film containing the thermoplastic resin A of the present invention as a main component, as measured by secondary ion mass spectrum, is not particularly limited.
In particular, when the ratio is 1/50 or less, the friction coefficient and the scratch resistance are further improved, which is particularly preferable.

【0022】本発明の熱可塑性樹脂Aを主成分とするフ
ィルムの厚さは0.5〜3μm、好ましくは0.5〜1
μmであることが必要である。フィルム厚さが上記の範
囲より小さいと耐ダビング性、摩擦係数が不良となり逆
に大きいと耐スクラッチ性が不良となるので好ましくな
い。本発明の熱可塑性樹脂Aを主成分とするフィルムの
表面の平均突起高さは5〜500nm、好ましくは10
〜300nm、さらに好ましくは15〜200nmの範
囲である場合に耐スクラッチ性、耐ダビング性、摩擦係
数がより一層良好となるので特に望ましい。
The thickness of the film containing the thermoplastic resin A of the present invention as a main component is 0.5 to 3 μm, preferably 0.5 to 1 μm.
It needs to be μm . If the film thickness is smaller than the above range, the dubbing resistance and the coefficient of friction are poor, and if it is large, the scratch resistance is poor, which is not preferable. The average protrusion height of the surface of the film mainly containing the thermoplastic resin A of the present invention is 5 to 500 nm, preferably 10 to 500 nm.
When the thickness is in the range of from 300 to 300 nm, and more preferably in the range of from 15 to 200 nm, the scratch resistance, the dubbing resistance and the friction coefficient are further improved, which is particularly desirable.

【0023】本発明の熱可塑性樹脂Aを主成分とするフ
ィルムの平均突起間隔は6μm以下、好ましくは4μm
以下である場合に耐スクラッチ性、耐ダビング性、摩擦
係数がより一層良好となるので特に望ましい。
The average interval between protrusions of the film containing the thermoplastic resin A of the present invention as a main component is 6 μm or less, preferably 4 μm.
It is particularly desirable that the content be the following, since the scratch resistance, the dubbing resistance, and the friction coefficient are further improved.

【0024】本発明の熱可塑性樹脂Aを主成分とするフ
ィルム表面の中心線深さRpは特に限定されないが、R
pが180nm以下、特に160nm以下の場合に耐ダ
ビング性がより一層良好となるので特に望ましい。ま
た、上記Rpと最大高さRtの比、Rt/Rpが1.5
〜2.5、特に1.7〜2.3の場合に耐スクラッチ
性、耐ダビング性、摩擦係数がより一層良好となるので
特に望ましい。
The center line depth Rp of the film surface containing the thermoplastic resin A of the present invention as a main component is not particularly limited.
It is particularly desirable that p is 180 nm or less, particularly 160 nm or less, because the dubbing resistance is further improved. Further, the ratio of Rp to the maximum height Rt, Rt / Rp is 1.5
In the case of 2.52.5, especially 1.7〜2.3, scratch resistance, dubbing resistance and friction coefficient are further improved, which is particularly desirable.

【0025】本発明の熱可塑性樹脂Aを主成分とするフ
ィルムの表面の中心線平均粗さRaと最大高さRtの
比、Rt/Raが9.0以下、特に8.5以下の場合に
耐スクラッチ性、耐ダビング性、摩擦係数がより一層良
好となるので特に望ましい。
When the ratio of the center line average roughness Ra to the maximum height Rt of the surface of the film mainly composed of the thermoplastic resin A of the present invention, Rt / Ra, is 9.0 or less, especially 8.5 or less. This is particularly desirable because the scratch resistance, dubbing resistance, and coefficient of friction are further improved.

【0026】本発明フィルムは上述したように、構成す
る熱可塑性樹脂が結晶性あるいは溶融光学異方性である
ことがきわめて望ましいが、溶融等方性フィルムの場
合、結晶かパラメータΔTcgが25〜65℃である場
合に耐スクラッチ性、摩擦係数がより一層良好となるの
で特に望ましい。
As described above, it is highly desirable that the thermoplastic resin constituting the film of the present invention is crystalline or has a melt optical anisotropy. In the case of a melt isotropic film, the crystalline or parameter ΔTcg is 25 to 65. C. is especially desirable because the scratch resistance and the coefficient of friction are further improved.

【0027】なお熱可塑性樹脂Aがポリエステルの場合
には熱可塑性樹脂A面の厚さ方向屈折率が1.5以下の
場合に、耐スクラッチ性、耐ダビング性がより一層良好
となるので特に望ましい。
When the thermoplastic resin A is a polyester, the scratch resistance and the dubbing resistance are further improved when the thickness direction refractive index of the thermoplastic resin A surface is 1.5 or less, which is particularly preferable. .

【0028】本発明フィルムを構成する熱可塑性樹脂A
がポリエステルの場合はフィルムの固有粘度が0.60
以上、特に0.70以上の場合に耐スクラッチ性がより
一層良好となるので特に望ましい。
Thermoplastic resin A constituting the film of the present invention
Is polyester, the intrinsic viscosity of the film is 0.60
Above, especially when it is 0.70 or more, scratch resistance is further improved, which is particularly desirable.

【0029】本発明フィルムを構成する熱可塑性樹脂A
がポリエステルの場合はフィルム中の低分子成分含有量
が0.8重量%以下、特に0.5重量%以下の場合に耐
スクラッチ性がより一層良好となるので特に望ましい。
Thermoplastic resin A constituting the film of the present invention
Is particularly preferable when the content of the low-molecular component in the film is 0.8% by weight or less, particularly 0.5% by weight or less, since the scratch resistance is further improved.

【0030】次に本発明フィルムの製造方法について説
明する。
Next, a method for producing the film of the present invention will be described.

【0031】まず、熱可塑性樹脂Aに不活性粒子を含有
せしめる方法としては、熱可塑性樹脂がポリエステルの
場合には、ジオール成分であるエチレングリコールのス
ラリーの形で分散せしめ、このエチレングリコールを所
定のジカルボン酸成分と重合せしめるのが延伸破れな
く、本発明範囲の厚さと平均粒径の関係、含有量、望ま
しい範囲の配向状態のフィルムを得るのに有効である。
また、不活性粒子を含有するポリエステルの溶融粘度、
共重合成分などを調節して、その結晶化パラメータΔT
cgを40〜65℃の範囲にしておく方法は延伸破れな
く、本発明範囲の厚さと平均粒径の関係、含有量、望ま
しい範囲の配向状態、表層粒子濃度比、平均突起高さ、
Rt/Rp比、Rt/Ra比のフィルムを得るのに有効
である。
First, as a method for incorporating inert particles into the thermoplastic resin A, when the thermoplastic resin is a polyester, the thermoplastic resin A is dispersed in the form of a slurry of ethylene glycol as a diol component, and the ethylene glycol is dispersed in a predetermined amount. Polymerization with the dicarboxylic acid component is effective for obtaining a film having the relationship between the thickness and the average particle size, the content, and the desired state of orientation within the range of the present invention without stretching breakage.
Also, the melt viscosity of polyester containing inert particles,
By adjusting the copolymerization component and the like, its crystallization parameter ΔT
The method of keeping cg in the range of 40 to 65 ° C. does not cause stretching breakage, the relationship between the thickness and the average particle size in the range of the present invention, the content, the orientation state in a desirable range, the surface particle concentration ratio, the average projection height,
This is effective for obtaining a film having an Rt / Rp ratio and an Rt / Ra ratio.

【0032】また、不活性粒子のエチレングリコールの
スラリーを140〜200℃、特に180〜200℃の
温度で30分〜5時間、特に1〜3時間熱処理する方法
は延伸破れなく、本発明範囲の厚さと平均粒径の関係、
含有量、望ましい範囲の配向状態、表層粒子濃度比のフ
ィルムを得るのに有効である。
Further, the method of heat-treating a slurry of inert particles of ethylene glycol at a temperature of 140 to 200 ° C., particularly 180 to 200 ° C., for 30 minutes to 5 hours, especially 1 to 3 hours, does not cause stretching breakage and is within the scope of the present invention. Relationship between thickness and average particle size,
It is effective to obtain a film having a content, a desired orientation state, and a surface layer particle concentration ratio.

【0033】また、熱可塑性樹脂(ポリエステルも含め
て)に不活性粒子を含有せしめる方法として、粒子をエ
チレングリコール中で140〜200℃、特に180〜
200℃の温度で30分〜5時間、特に1〜3時間熱処
理した後、溶媒を水に置換したスラリーの形で熱可塑性
樹脂と混合し、ベント方式の2軸押出機を用いて混練し
て熱可塑性樹脂に練り込む方法も本発明範囲の厚さと平
均粒径の関係、含有量、望ましい範囲の配向状態、表層
粒子濃度比、平均突起高さ、Rt/Rp比、Rt/Ra
比のフィルムを得るのにきわめて有効である。
As a method of incorporating inert particles into a thermoplastic resin (including polyester), the particles may be prepared by mixing the particles in ethylene glycol at 140 to 200 ° C., particularly 180 to 200 ° C.
After heat treatment at a temperature of 200 ° C. for 30 minutes to 5 hours, particularly 1 to 3 hours, the mixture is mixed with a thermoplastic resin in the form of a slurry in which the solvent is replaced with water, and kneaded using a vented twin-screw extruder. The method of kneading in the thermoplastic resin is also within the range of the present invention, ie, the relationship between the thickness and the average particle size, the content, the orientation state in the desired range, the surface layer particle concentration ratio, the average protrusion height, the Rt / Rp ratio, and the Rt / Ra.
It is very effective in obtaining a film of a specific ratio.

【0034】粒子の含有量を調節する方法としては、上
記方法で高濃度マスターを作っておき、それを成膜時に
不活性粒子を実質的に含有しない熱可塑性樹脂で希釈し
て粒子の含有量を調節する方法が有効である。
As a method of adjusting the content of the particles, a high-concentration master is prepared in the above-described manner, and the master is diluted with a thermoplastic resin substantially free of inert particles at the time of film formation. The method of adjusting is effective.

【0035】かくして、不活性粒子を所定量含有するペ
レットを必要に応じて乾燥したのち、公知の溶融押出機
に供給し、熱可塑性樹脂の融点以上、分解点以下でスリ
ット状のダイからシート状に押出し、キャスティングロ
ール上で冷却固化せしめて未延伸フィルムを作る。この
場合、未延伸フィルムに押出し成形する時の、口金スリ
ット間隙/未延伸フィルム厚さの比を5〜30、好まし
くは8〜20の範囲にすることが、延伸破れなく本発明
範囲の厚さと平均粒径の関係、含有量の範囲、望ましい
範囲の配向状態、表層粒子濃度比、全反射ラマン結晶化
指数のフィルムを得るのに有効である。
Thus, the pellets containing a predetermined amount of the inert particles are dried as required, and then supplied to a known melt extruder. To form an unstretched film. In this case, when extruding into an unstretched film, the ratio of the die slit gap / the thickness of the unstretched film to be in the range of 5 to 30, preferably 8 to 20 is set to the range of the present invention without stretching breakage. It is effective for obtaining a film having a relationship between the average particle size, a range of the content, a desired range of orientation state, a surface particle concentration ratio, and a total reflection Raman crystallization index.

【0036】次にこの未延伸フィルムを二軸延伸し、二
軸配向せしめる。延伸方法としては、逐次二軸延伸法ま
たは同時二軸延伸法を用いることができる。ただし、最
初に長手方向、次に幅方向の延伸を行なう逐次二軸延伸
法を用い、長手方向の延伸を3段階以上に分けて、総縦
延伸倍率を3.5〜6.5倍で行なう方法は延伸破れな
く、本発明範囲の厚さと平均粒径の関係、含有量、望ま
しい範囲の配向状態、表層粒子濃度比のフィルムを得る
のに有効である。ただし、熱可塑性樹脂が溶融光学異方
性樹脂である場合は長手方向延伸倍率は1〜1.1倍が
適切である。長手方向延伸温度は熱可塑性樹脂の種類に
よって異なり一概には言えないが、通常、その1段目を
50〜130℃とし、2段目以降はそれより高くするこ
とが本発明範囲の厚さと平均粒径の関係、含有量、望ま
しい範囲の配向状態、平均突起高さ、表層粒子濃度比の
フィルムを得るのに有効である。長手方向延伸速度は5
000〜50000%/分の範囲が好適である。幅方向
の延伸方法としてはステンタを用いる方法が一般的であ
る。延伸倍率は、3.0〜5.0倍の範囲が適当であ
る。幅方向の延伸速度は、1000〜20000%/
分、温度は80〜160℃の範囲が好適である。次にこ
の延伸フィルムを熱処理する。この場合の熱処理温度は
170〜200℃、特に170〜190℃、時間は0.
5〜60秒の範囲が好適である。
Next, the unstretched film is biaxially stretched and biaxially oriented. As the stretching method, a sequential biaxial stretching method or a simultaneous biaxial stretching method can be used. However, using a sequential biaxial stretching method in which stretching in the longitudinal direction and then in the width direction is performed first, the stretching in the longitudinal direction is divided into three or more stages, and the total longitudinal stretching ratio is 3.5 to 6.5 times. The method is effective for obtaining a film having the relationship between the thickness and the average particle size within the range of the present invention, the content, the orientation state within the desired range, and the surface layer particle concentration ratio without breaking the stretch. However, when the thermoplastic resin is a molten optically anisotropic resin, the stretching ratio in the longitudinal direction is appropriately from 1 to 1.1 times. The stretching temperature in the longitudinal direction differs depending on the type of the thermoplastic resin, and cannot be generally described. However, it is usually 50 to 130 ° C. for the first stage and higher than the second stage. It is effective to obtain a film having a relation of particle size, content, orientation state in a desirable range, average projection height, and surface layer particle concentration ratio. The longitudinal stretching speed is 5
The range of 000 to 50,000% / min is suitable. As a stretching method in the width direction, a method using a stenter is generally used. The stretch ratio is suitably in the range of 3.0 to 5.0 times. The stretching speed in the width direction is 1000 to 20000% /
The temperature is preferably in the range of 80 to 160 ° C. Next, this stretched film is heat-treated. In this case, the heat treatment temperature is 170 to 200 ° C., particularly 170 to 190 ° C., and the time is 0.
A range from 5 to 60 seconds is preferred.

【0037】[0037]

【作用】本発明は含有する粒子の大きさとフィルム厚さ
の関係、含有量、フィルム厚さを特定範囲とした熱可塑
性樹脂フィルムとしたので、従来の溶融製膜/二軸延伸
プロセスでは得られない表面形態とすることができたた
め、本発明の効果が得られたものと推定される。
According to the present invention, a thermoplastic resin film having a relation between the size of the particles contained therein and the film thickness, the content, and the film thickness in a specific range is obtained, which can be obtained by the conventional melt film forming / biaxial stretching process. It is presumed that the effect of the present invention was obtained because the surface morphology could not be obtained.

【0038】[0038]

【物性の測定方法ならびに効果の評価方法】本発明の特
性値の測定法並びに効果の評価方法は次の通りである。
[Method for measuring physical properties and method for evaluating effects] The method for measuring characteristic values and the method for evaluating effects according to the present invention are as follows.

【0039】(1)粒子の平均粒径 フィルムからポリエステルをプラズマ低温灰化処理法
(たとえばヤマト科学製PR−503型)で除去し粒子
を露出させる。処理条件はポリエステルは灰化されるが
粒子はダメージを受けない条件を選択する。これをSE
M(走査型電子顕微鏡)で観察し、粒子の画像(粒子に
よってできる光の濃淡)をイメージアナライザー(たと
えばケンブリッジインストルメント製QTM900)に
結び付け、観察個所を変えて粒子数5000個以上で次
の数値処理を行ない、それによって求めた数平均径Dを
平均粒径とする。
(1) Average particle size of particles The polyester is removed from the film by a plasma low-temperature incineration method (for example, PR-503 manufactured by Yamato Scientific Co., Ltd.) to expose the particles. The processing conditions are selected such that the polyester is ashed but the particles are not damaged. This is SE
Observed with a scanning electron microscope (M), the image of the particles (shading of light generated by the particles) is linked to an image analyzer (for example, QTM900 manufactured by Cambridge Instrument). The processing is performed, and the number average diameter D obtained thereby is defined as the average particle diameter.

【0040】D=ΣDi /N ここで、Di は粒子の円相当径、Nは個数である。D = ΣDi / N where Di is the circle equivalent diameter of the particles and N is the number.

【0041】(2)粒子の含有量 ポリエステルは溶解し粒子は溶解させない溶媒を選択
し、粒子をポリエステルから遠心分離し、粒子の全体重
量に対する比率(重量%)をもって粒子含有量とする。
場合によっては赤外分光法の併用も有効である。
(2) Content of Particles A solvent in which the polyester is dissolved but the particles are not dissolved is selected, the particles are centrifuged from the polyester, and the ratio (% by weight) to the total weight of the particles is defined as the particle content.
In some cases, the combined use of infrared spectroscopy is also effective.

【0042】(3)結晶化パラメータΔTcg、融解熱 パーキンエルマー社製のDSC(示差走査熱量計)II
型を用いて測定した。DSCの測定条件は次の通りであ
る。すなわち、試料10mgをDSC装置にセットし、
300℃の温度で5分間溶融した後、液体窒素中に急冷
する。この急冷試料を10℃/分で昇温し、ガラス転移
点Tgを検知する。さらに昇温を続け、ガラス状態から
結晶化発熱ピーク温度をもって冷結晶化温度Tccとし
た。さらに昇温を続け、融解ピークから融解熱を求め
た。ここでTccとTgとの差(Tcc−Tg)を結晶
化パラメータΔTcgと定義する。
(3) Crystallization parameter ΔTcg, heat of fusion DSC (differential scanning calorimeter) manufactured by PerkinElmer II
It was measured using a mold. The measurement conditions of DSC are as follows. That is, 10 mg of a sample is set in a DSC device,
After melting at a temperature of 300 ° C. for 5 minutes, it is quenched in liquid nitrogen. The quenched sample is heated at a rate of 10 ° C./min, and the glass transition point Tg is detected. The temperature was further raised, and the crystallization exothermic peak temperature from the glassy state was taken as the cold crystallization temperature Tcc. The temperature was further increased, and the heat of fusion was determined from the melting peak. Here, the difference between Tcc and Tg (Tcc−Tg) is defined as a crystallization parameter ΔTcg.

【0043】(4)表面の分子配向(屈折率) ナトリウムD線(589nm)を光源として、アッベ屈
折率計を用いて測定した。マウント液にはヨウ化メチレ
ンを用い、25℃、65%RHにて測定した。ポリマの
二軸配向性は長手方向、幅方向、厚さ方向の屈折率をN
1 、N2 、N3とした時、(N1 −N2 )の絶対値が
0.07以下、かつ、N3 /[(N1 +N2 )/2]が
0.95以下であることをひとつの基準とできる。ま
た、レーザー型屈折計を用いて屈折率を測定しても良
い。さらに、この方法では測定が難しい場合は全反射レ
ーザーラマン法を用いることもできる。
(4) Molecular Orientation (Refractive Index) of the Surface Using a sodium D line (589 nm) as a light source, measurement was performed using an Abbe refractometer. The measurement was performed at 25 ° C. and 65% RH using methylene iodide as the mounting solution. The biaxial orientation of the polymer is determined by setting the refractive index in the longitudinal, width, and thickness directions to N.
1, when the N 2, N 3, the absolute value of (N 1 -N 2) is 0.07 or less, and, N 3 / [(N 1 + N 2) / 2] is 0.95 or less Can be used as one criterion. The refractive index may be measured using a laser refractometer. Further, when measurement is difficult by this method, a total reflection laser Raman method can be used.

【0044】レーザー全反射ラマンの測定は、Jobi
n−Yvon社製RamanorU−1000ラマンシ
ステムにより、全反射ラマンスペクトルを測定し、例え
ばPETの場合では、1615cm-1(ベンゼン環の骨
格振動)と1730cm-1(カルボニル基の伸縮振動)
のバンド強度比の偏光測定比(YY/XX比など。ここ
でYY:レーザーの偏光方向をYにしてYに対して平行
なラマン光検出、XX:レーザーの偏光方向をXにして
Xに対して平行なラマン光検出)が分子配向と対応する
ことを利用できる。ポリマの二軸配向性はラマン測定か
ら得られたパラメータを長手方向、幅方向屈折率に換算
して、その絶対値、差などから判定できる。この場合の
測定条件は次のとおりである。
The measurement of the laser total reflection Raman is measured by Jobi.
The total reflection Raman spectrum was measured with a Ramanor U-1000 Raman system manufactured by n-Yvon, and in the case of PET, for example, 1615 cm -1 (skeleton vibration of benzene ring) and 1730 cm -1 (stretching vibration of carbonyl group).
The polarization measurement ratio of the band intensity ratio (YY / XX ratio etc., where YY: Raman polarization direction of laser is set to Y and Raman light parallel to Y is detected, XX: Polarization direction of laser is set to X and X And parallel Raman light detection) correspond to the molecular orientation. The biaxial orientation of the polymer can be determined by converting the parameters obtained from the Raman measurement into the refractive index in the longitudinal direction and the width direction, and determining the absolute value, the difference, and the like. The measurement conditions in this case are as follows.

【0045】光源 アルゴンイオンレーザー(5145オングストローム) 試料のセッティング フィルム表面を全反射プリズムに圧着させ、レーザのプ
リズムへの入射角(フィルム厚さ方向との角度)は60
°とした。
Light source Argon ion laser (5145 angstroms) Sample setting The film surface is pressed against a total reflection prism, and the angle of incidence of the laser on the prism (the angle with the film thickness direction) is 60.
°.

【0046】検出機 PM:RCA31034/Photon Counti
ng System(Hamamatsu C123
0) (supply 1600V) 測定条件 SLIT 1000μm LASER 100mV GATE TIME 1.0sec SCAN SPEED 12cm-1/m
in SAMPLING INTERVAL 0.2cm-1 REPEAT TIME 6 (5)全反射ラマン結晶化指数 Jobin−Yvon社製Ramanor U−100
0ラマンシステムにより、全反射セマンスペクトルを測
定し、カルボニル基の伸縮振動である1730cm-1
半価幅をもって表面の全反射ラマン結晶化指数とした。
測定条件は次のとおりである。測定深さは、表面から5
00〜1000オングストローム程度である。
Detector PM: RCA31034 / Photon County
ng System (Hamamatsu C123
0) (supply 1600 V) Measurement conditions SLIT 1000 μm LASER 100 mV GATE TIME 1.0 sec SCAN SPEED 12 cm −1 / m
in SAMPLING INTERVAL 0.2 cm -1 REPEAT TIME 6 (5) Total reflection Raman crystallization index Ramanor U-100 manufactured by Jobin-Yvon
The total reflection seman spectrum was measured by a 0 Raman system, and the surface was defined as a total reflection Raman crystallization index with a half-value width of 1730 cm −1 , which is the stretching vibration of the carbonyl group.
The measurement conditions are as follows. Measurement depth is 5 from the surface
It is on the order of 00 to 1000 angstroms.

【0047】光源 アルゴンイオンレーザー(5145オングストローム) 試料のセッティング レーザー偏光(S偏光)とフィルム長手方向が平行とな
るようにフィルム表面を全反射プリズムに圧着させ、レ
ーザのプリズムへの入射角(フィルム厚さ方向との角
度)は60°とした。
Light source Argon ion laser (5145 angstroms) Sample setting The film surface was pressed against a total reflection prism so that the laser polarization (S-polarization) and the film longitudinal direction were parallel, and the angle of incidence of the laser on the prism (film thickness) (The angle with the vertical direction) was 60 °.

【0048】検出機 PM:RCA31034/Photon Counti
ng System(Hamamatsu C123
0) (supply 1600V) 測定条件 SLIT 1000μm LASER 100mV GATE TIME 1.0sec SCAN SPEED 12cm-1/m
in SAMPLING INTERVAL 0.2cm-1 REPEAT TIME 6 (6)表面突起の平均高さ 2検出器方式の操作型顕微鏡[ESM−3200、エリ
オニクス(株)製]と断面測定装置[PMS−1、エリ
オニクス(株)製]においてフィルム表面の平坦面の高
さを0として走査した時の突起の高さ測定値を画像処理
装置[IBAS2000、カールツァイス(株)製]に
送り、画像処理装置上にフィルム表面突起画像を再構築
する。次に、この表面突起画像で突起部分を2値化に得
られた個々の突起の面積から円相当径を求めこれをその
突起の平均径とする。また、この2値化された個々の突
起部分の中で最も高い値をその突起の高さとし、これを
個々の突起について求める。この測定を場所をかえて5
00回繰返し、突起個数を求め、測定された全突起につ
いてその高さの平均値を平均高さとした。また個々の突
起の高さデータをもとに、高さ分布の標準偏差を求め
た。また操作型電子顕微鏡の倍率は、1000〜800
0倍の間の値を選択する。なお、場合によっては、高精
度光干渉式3次元表面解析装置(WYKO社製TOPO
−3D、対物レンズ:40〜200倍、高解像度カメラ
使用が有効)を用いて得られる高さ情報を上記SEMの
値に読み替えて用いてもよい。
Detector PM: RCA31034 / Photon County
ng System (Hamamatsu C123
0) (supply 1600 V) Measurement conditions SLIT 1000 μm LASER 100 mV GATE TIME 1.0 sec SCAN SPEED 12 cm −1 / m
in SAMPLING INTERVAL 0.2 cm -1 REPEAT TIME 6 (6) Average height of surface protrusions 2 operation type operating microscope [ESM-3200, manufactured by Elionix Co., Ltd.] and cross-section measuring device [PMS-1, Elionix ( Of the film surface when scanning with the height of the flat surface of the film surface as 0, and sending the measured value to the image processing apparatus [IBAS2000, manufactured by Carl Zeiss Co., Ltd.]. Reconstruct the projection image. Next, a circle-equivalent diameter is determined from the area of each of the protrusions obtained by binarizing the protrusions in the surface protrusion image, and this is defined as the average diameter of the protrusion. The highest value among the binarized individual projections is defined as the height of the projection, and this is determined for each individual projection. Change this measurement to 5
The process was repeated 00 times, and the number of protrusions was obtained. The average value of the heights of all the measured protrusions was defined as the average height. The standard deviation of the height distribution was determined based on the height data of each projection. The magnification of the operation type electron microscope is 1000 to 800.
Choose a value between 0x. In some cases, a high-precision optical interference type three-dimensional surface analyzer (TOPO manufactured by WYKO) may be used.
-3D, objective lens: 40 to 200 times, use of a high-resolution camera is effective), and the height information obtained by using the above-mentioned SEM value may be used.

【0049】(7)中心線平均表面粗さRa、中心線深
さRp、最大高さRt、突起間隔Sm小坂研究所製の高
精度薄膜段差測定器ET−10を用いて測定した。条件
は下記のとおりであり、20回の測定の平均値をもって
値とした。
(7) Center line average surface roughness Ra, center line depth Rp, maximum height Rt, protrusion interval Sm Measured using a high-precision thin film step measuring device ET-10 manufactured by Kosaka Laboratory. The conditions were as follows, and the value was determined as the average value of 20 measurements.

【0050】・触針先端半径:0.5μm ・触針荷重 :5mg ・測定長 :1mm ・カットオフ値:0.08mm なお、Ra、Rp、Rt、Smの定義は、たとえば、奈
良治郎著「表面粗さの測定・評価法」(総合技術センタ
ー、1983)に示されているものである。
• Tip radius of the stylus: 0.5 μm • Load of the stylus: 5 mg • Measurement length: 1 mm • Cut-off value: 0.08 mm The definitions of Ra, Rp, Rt, and Sm are described in, for example, Jiro Nara Measurement and Evaluation Method of Surface Roughness ”(General Technology Center, 1983).

【0051】(8)ヤング率 JIS−Z−1702に規定された方法にしたがって、
インストロンタイプの引っ張り試験機を用いて、25
℃、65%RHにて測定した。
(8) Young's modulus According to the method specified in JIS-Z-1702,
Using an Instron type tensile tester, 25
It measured at 65 degreeC and 65% RH.

【0052】(9)固有粘度[η](単位はdl/g) オルソクロルフェノール中、25℃で測定した溶液粘度
から下記式から計算される値を用いる。
(9) Intrinsic viscosity [η] (unit: dl / g) A value calculated from the following equation from the solution viscosity measured at 25 ° C. in orthochlorophenol is used.

【0053】すなわち、 ηsp/C=[η]+K[η]2 ・C ここで、ηsp=(溶液粘度/溶媒粘度)−1、Cは溶媒
100mlあたりの溶解ポリマ重量(g/100ml、
通常1.2)、Kはハギンス定数(0.343とす
る)。また、溶液粘度、溶媒粘度はオストワルド粘度計
を用いて測定した。
That is, η sp / C = [η] + K [η] 2 · C, where η sp = (solution viscosity / solvent viscosity) −1, and C is the weight of dissolved polymer per 100 ml of solvent (g / 100 ml,
Usually 1.2), K is a Haggins constant (0.343). The solution viscosity and the solvent viscosity were measured using an Ostwald viscometer.

【0054】(10)表層粒子濃度比 2次イオンマススペクトル(SIMS)を用いて、フィ
ルム中の粒子に起因する元素の内のもっとも高濃度の元
素とポリエステルの炭素元素の濃度比を粒子濃度とし、
厚さ方向の分析を行なう。SIMSによって測定される
最表層粒子濃度(深さ0の点)における粒子濃度Aとさ
らに深さ方向の分析を続けて得られる最高濃度Bの比、
A/Bを表層濃度比と定義した。測定装置、条件は下記
のとおりである。
(10) Surface Particle Concentration Ratio Using secondary ion mass spectroscopy (SIMS), the concentration ratio between the highest concentration element among the elements originating from the particles in the film and the carbon element of the polyester is defined as the particle concentration. ,
An analysis in the thickness direction is performed. The ratio of the particle concentration A at the outermost layer particle concentration (point at a depth of 0) measured by SIMS to the maximum concentration B obtained by continuing the analysis in the depth direction,
A / B was defined as the surface concentration ratio. The measuring device and conditions are as follows.

【0055】 測定装置 2次イオン質量分析装置(SIMS) 西独、ATOMIKA社製 A−DIDA3000 測定条件 1次イオン種:O2 + 1次イオン加速電圧:12KV 1次イオン電流:200nA ラスター領域:400μm□ 分析領域:ゲート30% 測定真空度:6.0×10-9Torr E−GUN:0.5KV−3.0A (11)単一粒子指数 フィルムの断面を透過型電子顕微鏡(TEM)で写真観
察し、粒子を検知する。観察倍数を100000倍程度
にすれば、それ以上分けることができない1個の粒子が
観察できる。粒子の占める全面積をA、その内2個以上
の粒子が凝集している凝集体の占める面積をBとした
時、(A−B)/Aをもって、単一粒子指数とする。T
EM条件は下記のとおりであり1視野面積:2μm2
測定を場所を変えて、500視野測定する。
Measurement device Secondary ion mass spectrometer (SIMS) A-DIDA3000 manufactured by Atomika, West Germany Measurement conditions Primary ion species: O 2 + Primary ion acceleration voltage: 12 KV Primary ion current: 200 nA Raster area: 400 μm □ Analysis area: Gate 30% Measurement vacuum degree: 6.0 × 10 −9 Torr E-GUN: 0.5 KV-3.0 A (11) Single particle index The cross section of the film is observed with a transmission electron microscope (TEM). And detect the particles. If the observation magnification is set to about 100,000, one particle that cannot be further divided can be observed. When the total area occupied by the particles is A, and the area occupied by the aggregate in which two or more particles are agglomerated is B, (AB) / A is defined as the single particle index. T
The EM conditions are as follows, and one visual field area: 2 μm 2 , measuring 500 visual fields at different locations.

【0056】・装置:日本電子製JEM−1200EX ・観察倍率:100000倍 ・加速電圧:100kV ・切片厚さ:約1000オングストローム (12)粒径比 上記(1)の測定において個々の粒子の長径の平均値/
短径の平均値の比である。
Apparatus: JEM-1200EX manufactured by JEOL Ltd. Observation magnification: 100,000 times Acceleration voltage: 100 kV Section thickness: about 1000 angstroms (12) Particle size ratio Average value/
It is the ratio of the average value of the minor axis.

【0057】すなわち、下式で求められる。That is, it is obtained by the following equation.

【0058】長径=ΣD1i /N 短径=ΣD2i /N D1i 、D2i はそれぞれ個々の粒子の長径(最大
径)、短径(最短径)、Nは総個数である。
[0058] major axis = ΣD1 i / N long diameter short diameter = ΣD2 i / N D1 i, D2 i each individual particle (maximum diameter), short diameter (the shortest diameter), N is the total number.

【0059】(13)粒径の相対標準偏差 上記(1)の方法で測定された個々の突起径Di 、平均
径D、粒子総数Nから計算される標準偏差σ
(13) Relative standard deviation of particle diameter Standard deviation σ calculated from individual projection diameter D i , average diameter D, and total number N of particles measured by the method of (1).

【0060】[0060]

【式1】 を平均径Dで割った値(σ/D)で表わした。(Equation 1) Is divided by the average diameter D (σ / D).

【0061】(14)低分子成分含有量 試料ポリマを粉砕しソックスレー抽出器を用いて、クロ
ロホルムを溶媒として、還流下で24時間抽出を行な
う。クロロホルムを蒸発させて得られた抽出物の重量を
もとの試料の重量に対する比率(重量%)をもって低分
子成分含有量とした。
(14) Low molecular component content The sample polymer is pulverized and extracted with chloroform using a Soxhlet extractor under reflux for 24 hours. The weight of the extract obtained by evaporating the chloroform was taken as the ratio (% by weight) to the weight of the original sample as the content of the low molecular component.

【0062】(15)結晶化促進係数 上記(3)の方法で粒子を1重量%含有するポリエステ
ルのΔTcg(I)、およびこれから粒子を除去した同
粘度のポリエステルのΔTcg(II)を測定し、ΔT
cg(II)とΔTcg(I)の差[ΔTcg(II)
−ΔTcg(I)]をもって、結晶化促進係数とした。
(15) Crystallization Acceleration Coefficient ΔTcg (I) of a polyester containing 1% by weight of particles by the method of (3) and ΔTcg (II) of a polyester having the same viscosity from which particles were removed were measured. ΔT
The difference between cg (II) and ΔTcg (I) [ΔTcg (II)
−ΔTcg (I)] as the crystallization promotion coefficient.

【0063】(16)フィルムの厚さ フィルムの厚さは、公知の方法、例えばダイヤルゲージ
法、光干渉法、重量法、薄膜段差測定法等によって求め
ることができる。
(16) Film Thickness The thickness of the film can be determined by a known method, for example, a dial gauge method, an optical interference method, a gravimetric method, a thin film step measurement method, or the like.

【0064】(17)耐スクラッチ性 フィルムを幅1/2インチのテープ状にスリットしたも
のをテープ走行性試験機を使用して、ガイドピン(表面
粗度:Raで100nm)上を走行させる(走行速度1
000m/分、走行回数10パス、巻き付け角:60
°、走行張力:20g)。この時、フィルムに入った傷
を顕微鏡で観察し、幅2.5μm以上の傷がテープ幅あ
たり2本未満は優、2本以上10本未満は良、10本以
上は不良と判定した。優が望ましいが、良でも実用的に
は使用可能である。
(17) Scratch resistance A film obtained by slitting a film into a tape having a width of 1/2 inch is run on guide pins (surface roughness: 100 nm in Ra) using a tape running tester ( Running speed 1
000m / min, number of runs 10 passes, winding angle: 60
°, running tension: 20 g). At this time, the scratches in the film were observed with a microscope, and if the number of scratches with a width of 2.5 μm or more was less than 2 per tape width, it was judged as excellent. Although excellent is desirable, even good is practically usable.

【0065】(18)耐ダビング性 フィルムに下記組成の磁性塗料をグラビヤロールにより
塗布し、磁気配向させ、乾燥させる。さらに、小型テス
トカレンダー装置(スチールロール/ナイロンロール、
5段)で、温度:70℃、線圧:200kg/cmでカ
レンダー処理した後、70℃、48時間キュアリングす
る。上記テープ原反を1/2インチにスリットし、パン
ケーキを作成した。このパンケーキから長さ250mの
長さをVTRカセットに組み込みVTRカセットテープ
とした。
(18) Dubbing resistance The film is coated with a magnetic paint having the following composition by a gravure roll, magnetically oriented, and dried. In addition, a small test calendar device (steel roll / nylon roll,
After performing a calendering process at a temperature of 70 ° C. and a linear pressure of 200 kg / cm, curing is performed at 70 ° C. for 48 hours. The raw tape was slit into 1/2 inch to prepare a pancake. A length of 250 m from this pancake was incorporated into a VTR cassette to form a VTR cassette tape.

【0066】 (磁性塗料の組成) ・Co含有酸化鉄(BET値50m2 /g) :100重量部 ・エスレックA(積水化学製塩化ビニル/酢酸ビニル共重合体):10重量部 ・ニッポラン2304(日本ポリウレタン製ポリウレタンエラストマ) :10重量部 ・コロネートL(日本ポリウレタン製ポリイソシアネート) :5重量部 ・レシチン :1重量部 ・メチルエチルケトン :75重量部 ・メチルイソブチルケトン :75重量部 ・トルエン :75重量部 ・カーボンブラック :2重量部 ・ラウリン酸 :1.5重量部 このテープに家庭用VTRを用いてシバソク製のテレビ
試験波形発生器(TG7/U706)により100%ク
ロマ信号を記録し、その再生信号からシバソク製カラー
ビデオノイズ測定器(925D/1)でクロマS/Nを
測定しAとした。また上記と同じ信号を記録したマスタ
ーテープのパンケーキを磁界転写方式のビデオソフト高
速プリントシステム(たとえばソニーマグネスケール
(株)製のスプリンタ)を用いてAを測定したのと同じ
試料テープ(未記録)のパンケーキへダビングした後の
テープのクロマS/Nを上記と同様にして測定し、Bと
した。このダビングによるクロマS/Nの低下(A−
B)が3dB未満の場合は耐ダビング性:優、3dB以
上5dB未満の場合は良、5dB以上は不良と判定し
た。優が望ましいが、良でも実用的には使用可能であ
る。
(Composition of magnetic paint) Co-containing iron oxide (BET value 50 m 2 / g): 100 parts by weight Eslek A (vinyl chloride / vinyl acetate copolymer manufactured by Sekisui Chemical): 10 parts by weight Nipporan 2304 ( Polyurethane elastomer manufactured by Nippon Polyurethane): 10 parts by weight Coronate L (polyisocyanate manufactured by Nippon Polyurethane): 5 parts by weight Lecithin: 1 part by weight Methyl ethyl ketone: 75 parts by weight Methyl isobutyl ketone: 75 parts by weight Toluene: 75 parts by weight • Carbon black: 2 parts by weight • Lauric acid: 1.5 parts by weight A 100% chroma signal was recorded on this tape by using a TV test waveform generator (TG7 / U706) manufactured by Shibasoku using a home VTR, and the reproduced signal was recorded. Chroma S with Shibasoku color video noise measuring instrument (925D / 1) To measure the N was A. The same sample tape (not yet measured) was obtained by measuring the pancake of the master tape recording the same signal as above using a magnetic field transfer type video software high-speed printing system (for example, a Sprinter manufactured by Sony Magnescale Co., Ltd.). The chroma S / N of the tape after dubbing to the pancake of (Recording) was measured in the same manner as described above, and was designated as B. Reduction of chroma S / N by this dubbing (A-
When B) was less than 3 dB, the anti-dubbing property was excellent. When it was 3 dB or more and less than 5 dB, it was judged as good, and when 5 dB or more was bad. Although excellent is desirable, even good is practically usable.

【0067】(19)摩擦係数μk フィルムを幅1/2インチのテープ状にスリットしたも
のをテープ走行試験機TBT−300型((株)横浜シ
ステム研究所製)を使用し、60℃、80%RH雰囲気
で走行させ、初期の摩擦係数を下記の式より求めた(フ
ィルム幅は1/2インチとした)。
(19) Coefficient of friction μk A film obtained by slitting a film into a tape having a width of 1/2 inch was used at 60 ° C. and 80 ° C. using a tape running tester TBT-300 type (manufactured by Yokohama System Laboratory Co., Ltd.). After running in a% RH atmosphere, the initial coefficient of friction was determined by the following equation (the film width was イ ン チ inch).

【0068】μk=0.733iog(T2 /T1 ) ここでT1 は入側張力、T2 は出側張力である。カイド
径は6mmφであり、ガイド材質はSUS27(表面粗
度0.2S)、巻き付け角は180°、走行速度は3.
3cm/秒である。この測定によって得られたμkが
0.35以下の場合は摩擦係数:良好、0.35を越え
る場合は摩擦係数:不良と判定した。このμkはフィル
ムを磁気記録媒体、コンデンサ、包装用などの加工をす
る時のハンドリング性を左右する臨界点である。
Μk = 0.733 iog (T 2 / T 1 ) where T 1 is the incoming tension and T 2 is the outgoing tension. The guide diameter is 6 mmφ, the guide material is SUS27 (surface roughness 0.2S), the winding angle is 180 °, and the running speed is 3.
3 cm / sec. When μk obtained by this measurement was 0.35 or less, the coefficient of friction was determined to be good, and when μk exceeded 0.35, the coefficient of friction was determined to be poor. This μk is a critical point that affects the handling property when processing the film into a magnetic recording medium, a capacitor, packaging, and the like.

【0069】(20)耐削れ性 フィルムを幅1/2インチにテープ状にスリットしたも
のに片刃を垂直に押しあて、さらに0.5mm押し込ん
だ状態で20cm走行させる(走行張力:500g、走
行速度:6.7cm/秒)。この時片刃の先に付着した
フィルム表面の削れ物の高さを顕微鏡で読みとり、削れ
量とした(単位はμm)。少なくとも片面について、こ
の削れ量が10μm以下の場合は耐削れ性:良好、10
μmを越える場合は耐削れ性:不良と判定した。この削
れ量:10μmという値は、印刷工場やカレンダー工程
などの加工工程で、フィルム表面が削れることによっ
て、工程上、製品性能上のトラブルがおこるか否かを判
定するための臨界点である。
(20) Abrasion resistance The film was slit into a tape having a width of 1/2 inch, and one edge was pressed vertically, and the film was further pushed in by 0.5 mm and run for 20 cm (running tension: 500 g, running speed) : 6.7 cm / sec). At this time, the height of the shavings on the film surface attached to the tip of the single blade was read with a microscope, and the shaving amount was used (unit: μm). When at least one side has a shaving amount of 10 μm or less, the shaving resistance is good: 10
If it exceeds μm, the chipping resistance was determined to be poor. The value of the shaving amount: 10 μm is a critical point for determining whether or not a trouble in the process and product performance occurs due to the shaving of the film surface in a processing step such as a printing factory or a calendering step.

【0070】[0070]

【実施例】本発明を実施例に基づいて説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described based on embodiments.

【0071】実施例1〜4,比較例1〜2 平均粒径の異なるコロイダルシリカに起因するシリカ粒
子を含有するエチレングリコールを調整し、ナトリウム
含有量を粒子に対し0.02〜1.5重量%とした。こ
のエチレングリコールスラリーを190℃で1.5時間
熱処理した後、テレフタル酸ジメチルとエステル交換反
応後、重縮合し、コロイダルシリカに起因するシリカ粒
子を所定量含有するPETのペレットを作った。この
時、重縮合時間を調節し固有粘度を0.7とした。ま
た、実施例4、比較例2はPETとp−オキシ安息香酸
メチルの共重合体からなる溶融光学異方性ポリエステル
(出光石油化学製LCP100E)と、コロイダルシリ
カに起因するシリカ粒子を含有するエチレングリコール
スラリーを190℃で1.5時間熱処理した後溶媒を水
に置換したスラリーとを、ベント方式の2軸押出機を用
いて混練し、コロイダルシリカに起因するシリカ粒子を
所定量含有するポリマを作った。これらのペレットをそ
れぞれ180℃で3時間減圧乾燥(3Torr)し、押
出機に供給し、300℃で溶融し、静電印加キャスト法
を用いて表面温度30℃のキャスティング・ドラムに巻
きつけて冷却固化し未延伸フィルムを作った。この未延
伸フィルムを温度80℃にて長手方向に1〜4.5倍延
伸した。この延伸は2組ずつのロールの周速差で、延伸
段数を1〜4段階で変更して行なった。この一軸延伸フ
ィルムをステンタを用いて延伸速度2000%/分で1
00℃で幅方向に4.0倍延伸し、定長下で、190℃
にて5秒間熱処理し、厚さ0.5〜3μmの二軸配向フ
ィルムを得た。これらのフィルムの本発明のパラメータ
および性能は第1表に示したとおりであり、本発明のパ
ラメータが本発明範囲内である場合は耐スクラッチ性、
摩擦係数は優または良であるが、パラメータが本発明範
囲外である場合には耐スクラッチ性、摩擦係数を兼備し
たフィルムは得られないことがわかる。
Examples 1-4 and Comparative Examples 1-2 Ethylene glycol containing silica particles derived from colloidal silica having different average particle diameters was prepared, and the sodium content was adjusted to 0.02 to 1.5 wt. %. This ethylene glycol slurry was heat-treated at 190 ° C. for 1.5 hours, transesterified with dimethyl terephthalate, and polycondensed to produce PET pellets containing a predetermined amount of silica particles derived from colloidal silica. At this time, the intrinsic viscosity was adjusted to 0.7 by adjusting the polycondensation time. In Example 4 and Comparative Example 2, a melt optically anisotropic polyester (LCP100E manufactured by Idemitsu Petrochemical) composed of a copolymer of PET and methyl p-oxybenzoate, and ethylene containing silica particles derived from colloidal silica were used. The glycol slurry was heat-treated at 190 ° C. for 1.5 hours, and then kneaded with a slurry in which the solvent was replaced with water using a vented twin-screw extruder to obtain a polymer containing a predetermined amount of silica particles caused by colloidal silica. Had made. Each of these pellets was dried under reduced pressure (3 Torr) at 180 ° C. for 3 hours, fed to an extruder, melted at 300 ° C., wound around a casting drum having a surface temperature of 30 ° C. using an electrostatic application casting method, and cooled. Solidified to make an unstretched film. This unstretched film was stretched 1 to 4.5 times in the longitudinal direction at a temperature of 80 ° C. This stretching was carried out by changing the number of stretching stages in 1 to 4 stages by the peripheral speed difference between two sets of rolls. This uniaxially stretched film is stretched using a stenter at a stretching speed of 2000% / min.
Stretched 4.0 times in the width direction at 00 ° C, and 190 ° C under constant length
For 5 seconds to obtain a biaxially oriented film having a thickness of 0.5 to 3 μm. The parameters and performance of the present invention for these films are as shown in Table 1. When the parameters of the present invention are within the range of the present invention, scratch resistance,
Although the coefficient of friction is excellent or good, when the parameter is out of the range of the present invention, a film having both scratch resistance and coefficient of friction cannot be obtained.

【表1】 [Table 1]

【0072】[0072]

【発明の効果】本発明は、製法の工夫により、不活性粒
子を含有する熱可塑性樹脂を用いて、粒子の大きさとフ
ィルム厚さの関係、含有量、フィルム厚さを特定範囲と
したフィルムとしたので、耐スクラッチ性、摩擦係数が
優れたフィルムとなり、磁気記録媒体用に用いた時の耐
ダビング性に優れたフィルムが得られたものである。本
発明フィルムの用途は加工工程でのフィルム表面の傷が
加工工程上、製品性能上特に問題となる磁気記録媒体用
ベースフィルムとして特に有用である。
According to the present invention, a film having a specific range of the particle size and the film thickness, the content, and the film thickness is determined by using a thermoplastic resin containing an inert particle by devising a manufacturing method. As a result, a film having excellent scratch resistance and friction coefficient was obtained, and a film having excellent dubbing resistance when used for a magnetic recording medium was obtained. The use of the film of the present invention is particularly useful as a base film for a magnetic recording medium in which scratches on the film surface in the processing step are particularly problematic in the processing step and in product performance.

フロントページの続き (51)Int.Cl.6 識別記号 FI C08L 67:02 (58)調査した分野(Int.Cl.6,DB名) C08J 5/18 B29C 55/00 - 55/30Continuation of the front page (51) Int.Cl. 6 identification code FI C08L 67:02 (58) Investigated field (Int.Cl. 6 , DB name) C08J 5/18 B29C 55/00-55/30

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 熱可塑性樹脂Aと不活性粒子とを主成分
とするフィルムであって、該フィルム中に含有される不
活性粒子の平均粒径がフィルム厚さの0.1〜10倍、
該粒子の含有量が0.5〜50重量%であることを特徴
とする厚さ0.5〜3μmの磁気記録媒体用二軸配向熱
可塑性樹脂フィルム。
1. A film containing thermoplastic resin A and inert particles as main components, wherein the average particle size of the inert particles contained in the film is 0.1 to 10 times the film thickness,
A biaxially oriented thermoplastic resin film for a magnetic recording medium having a thickness of 0.5 to 3 μm, wherein the content of the particles is 0.5 to 50% by weight.
【請求項2】 熱可塑性樹脂Aが結晶性ポリエステルで
あり、かつ、熱可塑性樹脂Aを主成分とするフィルムの
表面の全反射ラマン結晶化指数が20cm-1以下である
ことを特徴とする請求項1記載の磁気記録媒体用二軸配
向熱可塑性樹脂フィルム。
2. The thermoplastic resin A is a crystalline polyester, and the total reflection Raman crystallization index of the surface of the film containing the thermoplastic resin A as a main component is 20 cm −1 or less. Item 6. The biaxially oriented thermoplastic resin film for a magnetic recording medium according to Item 1.
【請求項3】 熱可塑性樹脂Aを主成分とするフィルム
に含有される不活性粒子が粒径比1.0〜1.3の粒子
であることを特徴とする請求項1〜2のいずれかに記載
の磁気記録媒体用二軸配向熱可塑性樹脂フィルム。
3. The inactive particles contained in the film containing the thermoplastic resin A as a main component are particles having a particle size ratio of 1.0 to 1.3 . 6. The biaxially oriented thermoplastic resin film for a magnetic recording medium according to item 1.
【請求項4】 熱可塑性樹脂Aを主成分とするフィルム
に含有される不活性粒子の相対標準偏差が0.6以下で
あることを特徴とする請求項1〜3のいずれかに記載の
磁気記録媒体用二軸配向熱可塑性樹脂フィルム。
4. The magnet according to claim 1, wherein the relative standard deviation of the inert particles contained in the film containing the thermoplastic resin A as a main component is 0.6 or less. Biaxially oriented thermoplastic resin film for recording media.
JP6017499A 1988-06-08 1994-02-14 Biaxially oriented thermoplastic resin film Expired - Fee Related JP2827880B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6017499A JP2827880B2 (en) 1988-06-08 1994-02-14 Biaxially oriented thermoplastic resin film

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP63-141972 1988-06-08
JP14197288 1988-06-08
JP6017499A JP2827880B2 (en) 1988-06-08 1994-02-14 Biaxially oriented thermoplastic resin film

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP64000775A Division JPH0780282B2 (en) 1988-06-08 1989-01-05 Biaxially oriented thermoplastic resin film

Publications (2)

Publication Number Publication Date
JPH06256544A JPH06256544A (en) 1994-09-13
JP2827880B2 true JP2827880B2 (en) 1998-11-25

Family

ID=26354027

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6017499A Expired - Fee Related JP2827880B2 (en) 1988-06-08 1994-02-14 Biaxially oriented thermoplastic resin film

Country Status (1)

Country Link
JP (1) JP2827880B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4858818B2 (en) * 2004-02-17 2012-01-18 東レ株式会社 Biaxially oriented polyester film

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63108037A (en) * 1986-08-27 1988-05-12 Teijin Ltd Biaxially oriented polyester film
JPS6381022A (en) * 1986-09-25 1988-04-11 Teijin Ltd Biaxially oriented polyester film

Also Published As

Publication number Publication date
JPH06256544A (en) 1994-09-13

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